RTOG-0828
Closed to Accrual
Protocol Information
Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants
Pilot Project to Reduce Missing RTOG Quality of Life Data Via Electronic Web-Based Form Collection: A Companion Study for RTOG 0415 (A Phase III Randomized Study of Hypofractionated 3D-CRT/IMRT Versus Conventionally Fractionated 3D-CRT/IMRT in Patients wi
Principal Investigator
Status
Closed to Accrual
Date Closed To Accrual
December 10, 2009
Disease Site
Genitourinary [GU] Prostate
Phase
III
Developmental Therapeutics
No
Primary Objective
EPIC completion rate at 6 months. Completion rate is defined as completion of any part of the QOL forms.
Patient Population
Only English-literate patients enrolled on RTOG 0415 who consented to participate in the quality of life component of that study (at one of the specified institutions) and have an e-mail address are eligible for enrollment in this companion study.
Target Accrual
40
Protocol Document
Informed Consent
Patient Study Webpage
There is no available patient study webpage available for this trial at this time.
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